Chlorotrimethylsilane → HCID 89499943, compound

HRID 1527840Notes

Reaction equation

HRID 1527840 reaction equation
[Br:1][CH2:2][CH2:3][CH2:4][CH:5]=[CH2:6].[CH3:7][C@@:8]12[C@H:18]3[CH2:19][CH2:20][C@:21]4([CH3:31])[C@@:25]5([O:30]C(=O)CC5)[CH2:24][CH2:23][C@H:22]4[C@@H:17]3[CH:16]=[CH:15][C:14]1=[CH:13][C:11](=[O:12])[CH2:10][CH2:9]2.C[Si](Cl)(C)C>C(Cl)Cl.CCOCC>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C@@H:9]1[C@@:8]2([CH3:7])[C:14]([CH2:15][CH2:16][C@@H:17]3[C@@H:18]2[CH2:19][CH2:20][C@@:21]2([CH3:31])[C@H:22]3[CH2:23][CH2:24][C:25]2=[O:30])=[CH:13][C:11](=[O:12])[CH2:10]1

Participants

6

Procedure

Cp2ZrHCl (206 mg, 0.80 mmol, 2.0 eq.) was added to a stirred, room temperature, solution of 5-bromo-1-pentene (0.12 mL, 1.0 mmol, 2.5 eq.) in CH2Cl2 (0.40 mL) under an argon atmosphere. After stirring for about 15 min, the resulting clear yellow solution was transferred via syringe over about 1 min to a clear colourless stirred solution of CuOTf-ligand complex (30.0 mg, 0.040 mmol, 0.10 eq.) in Et2O (2.0 mL) under an argon atmosphere. The resulting dark mixture was allowed to stir for an additional 10 min before Canrenone (136.0 mg, 0.40 mmol, 1.0 eq.) and TMSCl (0.26 mL, 2.00 mmol, 5.0 eq.) were added sequentially dropwise via syringe. Stirring at room temperature was continued arbitrarily for 15 h before the reaction was quenched by the addition of Et2O (ca 3 mL) and NH4Cl (1 M aq., ca 1.5 mL). The mixture was partitioned between the aqueous and Et2O layers and the former phase was extracted with Et2O (3×10 mL). The combined organic phase was washed with NaHCO3 (sat. aq., ca 10 mL), dried (Na2SO4), filtered and concentrated in vacuo to give an oil. Flash column chromatography of the yellow residue (30:70 EtOAc/petrol; SiO2) gave major diastereomer (4) (+)-7α-(5-bromopentyl)-17α-hydroxy-3-oxo-pregn-4-ene-21-carboxylic acid γ-lactone (64 mg, 0.13 mmol, 33%) and minor diastereomer (4a) (+)-1α-(5-bromopentyl)-4-androstene-3,17-dione (14 mg, 0.028 mmol, 7%). Diastereomeric ratio was determined by integration of 1H NMR spectra.

Workup

  1. additionwere added sequentially dropwise via syringe
  2. stirringStirring at room temperature
  3. waitwas continued arbitrarily for 15 h before the reaction
  4. customwas quenched by the addition of Et2O (ca 3 mL) and NH4Cl (1 M aq., ca 1.5 mL)
  5. customThe mixture was partitioned between the aqueous and Et2O layers
  6. extractionthe former phase was extracted with Et2O (3×10 mL)
  7. washThe combined organic phase was washed with NaHCO3 (sat. aq., ca 10 mL)
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. customto give an oil

Sources & evidence

ORD record
ord-99992eb9badf4af6ac0deb0d8e3d697d
Source dataset
uspto-grants-2015_07
Patent number
US09090545B2

Reaction notes

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